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NC1P65SE
NEOCHILD, LLC · Model NC1P65SE · UDI-DI 10816336020172
KNT
Prescription
1
510(k) clearances
25,972
Adverse events (630 deaths)
268
Recalls
228
Facilities
Description
Feeding Tube 6.5 Fr. x 40 cm. - Polyurethane
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| 2026-04-30 | Avanos Medical, Inc. | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.